KIT FOR TESTING COVID-19 ANTIGEN AND METHOD FOR TESTING SAME

Abstract

Disclosed is a kit for testing a COVID-19 antigen. The kit includes a test card, a conjugate pad and a reaction pad being arranged on the test card; wherein the conjugate pad is provided with a labeled antibody Ab1 and a labeled antibody Ab3 of the COVID-19 antigen, and a quality control line and a test line are arranged in parallel with an interval on the reaction pad, the test line being provided with a coating antibody Ab2, and the quality control line being provided with a coating antibody Ab4. With the kit, by the AIE immunofluorescence chromatographic technique, the AIE fluorescent microspheres are used as labels, and the test result of the test card is directly determined and read by using a fluorescent flashlight, or the test result is read by using a fluorescent tester. Such kits have the advantages of high sensitivity, strong specificity and simple operation.

Claims

1. A kit for testing a coronavirus disease 2019 (COVID-19) antigen, comprising a test card, a conjugate pad and a reaction pad being arranged on the test card; wherein the conjugate pad is provided with a labeled antibody Ab1 and a labeled antibody Ab3 of the COVID-19 antigen, and a quality control line and a test line are arranged in parallel with an interval on the reaction pad, the test line being provided with a coating antibody Ab2, and the quality control line being provided with a coating antibody Ab4.

2. The kit according to claim 1, wherein the labeled antibody Ab1 is biologically derived from a murine monoclonal antibody IgG.

3. The kit according to claim 1, wherein the coating antibody Ab2 is biologically derived from a murine monoclonal antibody IgG.

4. The kit according to claim 1, wherein the labeled antibody Ab3 is biologically derived from a chicken antibody.

5. The kit according to claim 1, wherein the coating antibody Ab4 is biologically derived from a goat antibody.

6. The kit according to claim 1, wherein the labeled antibody Ab1 and the labeled antibody Ab3 both comprise AIE fluorescent microspheres.

7. The kit according to claim 1, wherein a final concentration of the labeled antibody Ab1 is 0.3 mg/ml, and a final concentration of the coating antibody Ab2 is 1 mg/mL.

8. The kit according to claim 1, wherein a final concentration of the labeled antibody Ab3 is 0.3 mg/ml, and a final concentration of the coating antibody Ab4 is 0.5 mg/mL.

9. The kit according to claim 1, further comprising a sample extraction solution for extracting a sample, an extraction bottle, and a disposable sampling swab.

10. The kit according to claim 9, wherein the sample extraction solution comprises 0.01 M BB, 1% PVP, 1% sodium chloride, and 1% Tween.

11. The kit according to claim 1, wherein the test card further comprises a sample pad, an absorbent pad, and a bottom plate; wherein the test card is formed by successively arranging, fixing and bonding the sample pad, the conjugate pad, the reaction pad, and the absorbent pad onto a surface of the bottom plate, wherein two ends of the reaction pad are respectively lapped with one end of the absorbent pad and one end of the conjugate pad, the other end of the conjugate pad is lapped with one end of the sample pad, the sample pad and the conjugate pad are respectively disposed on two ends of the bottom plate, and the quality control line and the test line are arranged on the reaction pad.

12. The kit according to claim 11, wherein the sample pad is prepared by: evenly applying a sample pad treatment solution to a 0.8-1.0 cm original sample pad by an amount of 3-4 mL/piece, and drying the sameat 55° C. for 6-8 h.

13. The kit according to claim 11, wherein sample pad treatment solution comprises 0.1 M BB, 1% sucrose, 1% trehalose, and 1% PVP K30.

14. The kit according to claim 11, wherein the sample pad is composed of a glass cellulose membrane.

15. The kit according to claim 11, wherein the absorbent pad is an H-1 absorbent paper.

16. The kit according to claim 11, wherein the bottom plate is a PVC sheet.

17. The kit according to claim 1, wherein a case is adaptively sleeved onto an outer surface of the test card; wherein the case comprises an observation window and a well.

18. The kit according to claim 1, wherein the test card further comprises a sample pad, an absorbent pad, and a bottom plate; wherein the test card is formed by successively arranging, fixing and bonding the sample pad, the conjugate pad, the reaction pad, and the absorbent pad onto a surface of the bottom plate, wherein two ends of the reaction pad are respectively lapped with one end of the absorbent pad and one end of the conjugate pad, the other end of the conjugate pad is lapped with one end of the sample pad, the sample pad and the conjugate pad are respectively disposed on two ends of the bottom plate, the quality control line and the test line are arranged on the reaction pad, the bottom plate is a PVC sheet,the sample pad is composed of a glass cellulose membrane, the absorbent pad is an H-1 absorbent paper, a case is adaptively sleeved onto an outer surface of the test card, wherein the case comprises an observation window and a well; the conjugate pad is provided with a labeled antibody Ab1 and a labeled antibody Ab3 of the COVID-19 antigen, and a quality control line and a test line are arranged in parallel with an interval on the reaction pad, the test line being provided with a coating antibody Ab2, the quality control line being provided with a coating antibody Ab4, the labeled antibody Ab1 comprises AIE fluorescent microspheres, and the labeled antibody Ab3 comprises AIE fluorescent microspheres; the labeled antibody Ab 1 is biologically derived from a murine monoclonal antibody IgG, the coating antibody Ab2 is biologically derived from a murine monoclonal antibody IgG, the labeled antibody Ab3 is biologically derived from a chicken antibody; and the coating antibody Ab4 is biologically derived from a goat antibody; a final concentration of the labeled antibody Ab1 0.3 mg/mL on the test card, a final concentration of the coating antibody Ab2 is 1 mg/mL on the test card, a final concentration of the labeled antibody Ab3 of the quality control line is 0.3 mg/mL on the test card, and a final concentration of the coating antibody Ab4 is 0.5 mg/mL on the test card; the kit further comprises a sample extraction solution for extracting a sample, an extraction bottle, and a disposable sampling swab, and the sample extraction solution comprises 0.01 M BB, 1% PVP, 1% sodium chloride, and 1% Tween.

19. A method for testing a coronavirus disease 2019 (COVID-19) antigen using a kit, the kit comprising a test card, a conjugate pad and a reaction pad being arranged on the test card; wherein the conjugate pad is provided with a labeled antibody Ab1 and a labeled antibody Ab3 of the COVID-19 antigen, and a quality control line and a test line are arranged in parallel with an interval on the reaction pad, the test line being provided with a coating antibody Ab2, and the quality control line being provided with a coating antibody Ab4; the method comprising: sampling an oral pharyngeal mucosa liquid by inserting a disposable sampling swab from a human oral cavity into a throat and slowly rotating and wiping bilateral pharyngeal tonsils and a posterior wall of pharynx; placing the sampling swab into an extraction bottle to which a sample extraction solution is added in advance, and sufficiently uniformly mixing the sample, such that the oral pharyngeal mucosa liquid remains in the extraction bottle; and dropwise adding the sampled oral pharyngeal mucosa liquid into the test card in the kit for testing, and determining a test result according to the test line and the quality control line.

20. A method for testing a coronavirus disease 2019 (COVID-19) antigen using a kit, the kit comprising a test card, a conjugate pad and a reaction pad being arranged on the test card; wherein the conjugate pad is provided with a labeled antibody Ab1 and a labeled antibody Ab3 of the COVID-19 antigen, and a quality control line and a test line are arranged in parallel with an interval on the reaction pad, the test line being provided with a coating antibody Ab2, and the quality control line being provided with a coating antibody Ab4; the method comprising: sampling a nasal mucosa fluid or an oral pharyngeal mucosa fluid by using a disposable sampling swab; placing the sampling swab into a single-lug tube to which a sample extraction solution is added in advance, and sufficiently uniformly mixing the sample, such that the nasal mucosa fluid or the oral pharyngeal mucosa fluid remains in the single-lug tube; and dropwise adding the sampled nasal mucosa fluid or oral pharyngeal mucosa fluid into the test card in the kit for testing, and determining a test result according to the test line and the quality control line.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] FIG. 1 is a schematic structural view of a test card in a kit according to the present disclosure; and

[0023] FIG. 2 is a schematic structural view of a case fitted to the test card according to the present disclosure.

DETAILED DESCRIPTION

[0024] Some exemplary embodiments of the present disclosure are described in detail hereinafter with reference to the accompanying drawings.

[0025] The AIE immunofluorescence chromatographic technique is a novel dry quantitative testing technique combining the AIE fluorescence technique and the traditional immunochromatographic technique. This technique not only has the advantages of simple operation, quick testing, and good portability of the colloidal gold immunochromatographic technique, but also achieves accuracy of a test result by the tracing enhancement technique of an aggregation-induced emission (AIE) material. Compared with the traditional fluorescence quick testing technique, this technical has merits of higher sensitivity, wider testing range, low cost, no background, and no quenching.

[0026] According to the present disclosure, in AIE immunofluorescence chromatographic technique, the content of the COVID-19 antigen in a nasal mucosa or oral pharyngeal mucosa fluid is tested by using the double antibody sandwich method. By means of process condition optimization, performance estimation, clinical application, and the like, an effective immunofluorescence chromatography-based kit for testing the COVID-19 antigen.

[0027] The present disclosure provides a kit for testing a COVID-19 antigen. The kit includes a test card, a disposable sampling swab, an extraction bottle, and a sample extraction solution disposed in a sample extraction solution bottle. A conjugate pad and a reaction pad are arranged on the test card; wherein the conjugate pad is provided with a labeled antibody Ab1 and a labeled antibody Ab3 of the COVID-19 antigen, and a quality control line and a test line are arranged in parallel with an interval on the reaction pad. The test line is provided with a coating antibody Ab2, and the quality control line is provided with a coating antibody Ab4.

[0028] The disposable sampling swab is configured to sample an oral pharyngeal mucosa fluid or a nasal mucosa fluid of a human body. The sampled mucosa fluid is placed into the sample extraction solution in the extraction bottle, and the fluid sample to be tested is uniformly mixed. Afterwards, the sample to be tested is dropwisely added to the test card, and a test result is determined and read by the test line and the quality control line.

[0029] The sample extraction solution mainly includes 0.01 M BB, 1% PVP, 1% sodium chloride, and 1% Tween.

[0030] In the test card, a biological origin of the labeled antibody of the COVID-19 antigen in the conjugate pad is as illustrated by Abl, and a biological origin of the coating antibody Ab2 of the COVID-19 antigen in the reaction pad is as illustrated by Ab2, a biological origin of the labeled antibody of the quality control line in the conjugate pad is as illustrated by Ab3, and a biological origin of the coating antibody of the quality control board in the reaction pad is as illustrated by Ab4. The details are as listed in Table 1.

TABLE-US-00001 TABLE 1 Testing of antibodies of COVID-19 antigen, and biological origin of antigen Main materials Biological origin Labeled antibody Ab1 of COVID-19 antigen Murine monoclonal antibody IgG Coating antibody Ab2 of COVID-19 antigen Murine monoclonal antibody IgG Chicken IgY labeled antibody Ab3 Chicken antibody Goat anti-chicken IgY coating antibody Ab4 Goat antibody

[0031] Further, the labeled antibody Ab 1 contains AIE fluorescent microspheres (that is, an AIE fluorescently labeled antibody or an AIE fluorescent label), and the labeled antibody Ab3 contains AIE fluorescent microspheres (that is, an AIE fluorescently labeled antibody or an AIE fluorescently labeled antibody).

[0032] Preferably, a final concentration of the labeled antibody Ab1 0.3 mg/mL on the test card, a final concentration of the coating antibody Ab2 is 1 mg/mL on the test card, a final concentration of the labeled antibody Ab3 of the quality control line is 0.3 mg/mL on the test card, and a final concentration of the coating antibody Ab4 is 0.5 mg/mL on the test card.

[0033] During use of the test card, under chromatography of a capillary effect, the COVID-19 antigen in the sample is conjugated to the AIE fluorescently labeled antibody on the test card and is spread to the test region and captured by a COVID-19 monoclonal antibody coated by the test line, and hence an “antibody-antigen-fluorescent antibody” complex is formed. In the meantime, a concentration of the COVID-19 antigen is proportional to a fluorescence intensity of the complex, and negative and positive may be directly determined using a fluorescent flashlight.

[0034] As illustrated in FIG. 1, a test card 10 further includes a sample pad 11, an absorbent pad 14, and a bottom plate 15. The bottom plate 15 is configured to an elongated strip. The test card 10 is formed by successively arranging, fixing and bonding the sample pad 11, a conjugate pad 12, a reaction pad 13, and the absorbent pad 14 onto a surface of the bottom plate 15. Two ends of the reaction pad 13 are respectively lapped with one end of the absorbent pad 14 and one end of the conjugate pad 12, the other end of the conjugate pad 12 is lapped with one end of the sample pad 11, the sample pad 11 and the absorbent pad 14 are respectively disposed on two ends of the bottom plate 15, and a quality control line (C line) 16 and a test line (T line) 17 are arranged on the reaction pad 13.

[0035] Further, as illustrated in FIG. 2, a case 20 is adaptively sleeved onto an outer surface of the test card 10; wherein the case 20 includes an observation window 22 and a well 21. The case 20 is made of a rigid material, for example, a rigid paper, a PVC, or the like. After the test card 10 is assembled into the case 20, the sample pad 11 is correspondingly arranged at the position of the well 21, and the reaction pad 12 is correspondingly arranged at the position of the observation window 22. Since the test card 10 is soft, the test operation is inconvenient. The case 20 is mainly to facilitate testing by using the test card 10, and strengthen rigidity of the test card 10, to ensure uprightness of the test card 10 during testing and prevent the test card 10 from being bent which affects the testing.

[0036] Further, during manufacturing, for protection of the test card 10 from moisture or contaminants, generally, the test card 10 assembled into the case 20 and a desiccant are packaged in a sealed fashion with an aluminum foil.

[0037] In the test card 10:

[0038] The sample pad 11 is mainly composed of a glass cellulose membrane.

[0039] The conjugate pad 12 is mainly composed of a glass cellulose membrane, and the conjugate pad 12 is provided with a labeled antibody Ab1 with an AIE fluorescent label, and a labeled antibody Ab3 with an AIE fluorescent label. The labeled antibody Ab1 is a COVID-19 antibody Ab 1, and the labeled antibody Ab3 is a chicken IgY antibody Ab3.

[0040] The reaction pad 13 is composed of a nitrocellulose (NC) membrane. The test line is coated with the antibody Ab2, that is, coated with the COVID-19 monoclonal antibody Ab2; and the quality control line is coated with the antibody Ab4, that is, coated by the goat anti-chicken IgY antibody.

[0041] The absorbent pad 14 is an H-1 absorbent paper.

[0042] The bottom plate 15 is a PVC sheet.

[0043] The present disclosure further provides a method for sampling a COVID-19 antigen. The method employs the kit as described above for testing the COVID-19 antigen. The method includes sampling using an oral pharyngeal swab and sampling using a nasal pharyngeal swab.

[0044] Oral pharyngeal swab: A sampling swab is totally inserted from a human oral cavity into a throat, and is slowly rotated to wipe bilateral pharyngeal tonsils while avoiding contact with the tongue.

[0045] Nasal pharyngeal swab: a distance from a nose tip to an ear lobe is measured and the distance is marked with the finger, and a sampling swab is inserted into a nasal cavity along a direction perpendicular the nose (face) to a depth of half of a length from the ear lobe to the nose tip. In the advent of a resistance, the swab reaches the nasal pharyngeal. In this case, the sampling swab is maintained at the nasal pharyngeal for 15 to 30 s, and is slightly rotated for 3 to 5 times and then slowly taken out.

[0046] Sample storage: The collected sample shall be immediately subjected to testing. If the sample collected by the sampling swab is not immediately tested, the sample shall be immediately placed in a dry, disinfected and sealed plastic tube for storage.

[0047] Upon sample collection, the sample shall be immediately treated using the sample extraction solution provided by the kit. The treated sample may be preserved for 2 h under room temperatures, 3 h under temperatures of 2 to 8° C., and for 2 months under temperatures of −20±5° C. Note: The sample subjected to refrigeration preservation shall be restored to the room temperatures and then tested.

[0048] The sampling specifically includes the following steps:

[0049] opening a dropper bottle, and vertically dropwise adding 11 drops (about 400 μL) of the sample extraction solution into the extraction bottle;

[0050] sample collection: collecting the sample using an oral pharyngeal swab or a nasal pharyngeal swab;

[0051] upon sampling, placing the disposable sampling swab into the extraction bottle containing the sample extraction solution, soaking the swab in the sample extraction solution and extrusively rotating the swab for 10 times to sufficiently mix the sample, and then extruding the swab over the surface of the solution such that the fluid in the swab remains in the tube as much as possible;

[0052] connecting a disposable dropper to the extraction bottle containing the sample extraction solution;

[0053] opening an aluminum foil bag, taking out the test card, and placing the test card on a dry and clean platform;

[0054] vertically dropwise adding the solution in the extraction bottle into the well in the test card, wherein due to operation differences, if, 2 min after 3 drops of the sample extraction solution is added, it is found through the observation window that no solution layer is precipitated, 1 more drop of the sample extraction solution is added to the corresponding well under the observation window; and

[0055] within 10 to 15 min after sampling adding, determining and reading the test result on the test line and the quality control line by irradiating the observation window with the fluorescent flashlight, wherein the test result displayed after 30 min is of no clinical significance.

EXAMPLE 1

Preparation of Kit

[0056] 1. Preparation of the Test Card

[0057] Step 1: Preparation of the Conjugate Pad

[0058] AIE fluorescence activation: 100 μL of AIE fluorescent microspheres were added to 800 μL of IVIES (2-morpholineethanesulfonic acid) in a centrifuge tube and sonicated for 3 min. 30 μL of EDC (1-ethyl-carbodiimide hydrochloride) and NHS (N-hydroxysuccinimide) (1:1) activation solution was measured and mixed in the centrifuge tube, sonicated until it was evenly dispersed, equilibrated at room temperatures for a period of time, and centrifuged at 4° C. for 15 min at 12000 r/min, and a supernatant was removed.

[0059] Antibody conjugation: 1 mL MES was added to the centrifuge tube, and sonicated for 3 min after vortexing, 0.3 mg of COVID-19 antibody was added and rotated for coupling reaction for 2 h, and after static placement for 5 min, 0.3 mg of chicken IgY antibody was added.

[0060] Closure and preservation: 100 μL of 10% BSA (bovine serum albumin) solution was added to the centrifuge tube and preserved for 30 min, and was centrifuged at 12000 r/min at 4° C. for 15 min. The supernatant was removed, 1 mL of Tris buffer (Tris(hydroxymethyl)aminomethane) was added, sonicated for 3 min, and followed by centrifugation at 12000 r/min at 4° C. for 15 min. The operation was repeated once. 1 mL of microsphere compound solution was added after the supernatant was moved, sonicated for 3 min, centrifuged at 2000 r/min for 3 min; and the precipitate was removed and kept at 4 ° C. without irradiation from light.

[0061] Conjugate pad: A prepared fluorescent microparticle solution was uniformly sprayed on a glass fiber of 1.5-1.8 cm at a rate of 6 μL/cm, and dried at 55° C. for 3 to 4 h.

[0062] Step 2: Preparation and Treatment of the Sample Pad

[0063] Preparation of a treatment solution: 0.1 M BB, 1% sucrose, 1% trehalose, and 1% PVP K30 (polyvinylpyrrolidone).

[0064] Treatment of the sample pad: the treatment solution is evenly applied to a 0.8-1.0 cm sample pad by an amount of 3-4 mL/piece (width: 17-18, length: 30 cm), and dried at 55° C. for 6-8 h.

[0065] Step 3: Preparation of the Reaction Pad

[0066] Preparation of a coating solution: 0.05 M Tris (Tris(hydroxymethyl)aminomethane), and 1% sucrose. Scoring:

[0067] 1) Test line: A reaction pad (that is, a nitrocellulose membrane, NC membrane) was pasted on the bottom plate (a PVC sheet), a COVID-19 coating antibody Ab2 was prepared with the coating solution at a concentration of 1 mg/mL, uniformly sprayed on the nitrocellulose membrane at 1.2 μL/cm using a quantitative film-spraying instrument, and dried in an air-blowing drying oven at 50° C. for 24 hours to prepare a reaction pad containing the test line;

[0068] 2) Quality control line: A coating antibody Ab4 of goat anti-chicken IgY with a concentration of 0.5 mg/mL was uniformly sprayed on the reaction pad containing the test line using a quantitative film sprayer at a concentration of 1.0 μL/cm, and dried in a blast drying oven at 50° C. for 24 h to prepare a reaction pad containing the test line and the quality control line.

[0069] Step 4: Assembly of the test card: The treated sample pad, conjugate pad and absorbent pad were successively attached to the PVC sheet, and the assembled PVC sheet is cut into an immunochromatographic test card with a width of 3.85 mm by a strip cutter.

[0070] 2. Sample Testing and Result Determination

[0071] Preparation of a sample extraction solution: 0.01 M BB, 1% PVP (polyvinylpyrrolidone), 1% sodium chloride, and 1% Tween.

[0072] Sample Testing:

[0073] opening a dropper bottle, and vertically dropwise adding 11 drops (about 400 μL) of the sample extraction solution into the extraction bottle;

[0074] sample collection: collecting the sample using an oral pharyngeal swab or a nasal pharyngeal swab;

[0075] upon sampling, placing the disposable sampling swab into the extraction bottle containing the sample extraction solution, soaking the swab in the sample extraction solution and extrusively rotating the swab for 10 times to sufficiently mix the sample, and then extruding the swab over the surface of the solution such that the fluid in the swab remains in the tube as much as possible;

[0076] connecting a disposable dropper to the extraction bottle containing the sample extraction solution;

[0077] opening an aluminum foil bag, taking out the test card, and placing the test card on a dry and clean platform; and

[0078] vertically dropwise adding the solution in the extraction bottle into the well in the test card, wherein due to operation differences, if, 2 min after 3 drops of the sample extraction solution is added, it is found through the observation window that no solution layer is precipitated, 1 more drop of the sample extraction solution is added to the corresponding well under the observation window; and determining and reading the test result 15 min later with the fluorescent flashlight. In the fluorescence test, no matter whether it is negative or positive, the quality control line shall show a fluorescence band, and in this case, it is proved that the test result is valid.

[0079] 3. Packaging of the Kit

[0080] The composition, packaging and quantity (25 pieces/kit) of the COVID-19 antigen kit in human oral pharyngeal or nasal pharyngeal samples are listed in Table 2.

TABLE-US-00002 TABLE 2 Composition, packaging and quantity of the kit Serial Specification number Component Main component (μL) Quantity 1 Test card for the This product is composed of a For one person 25 COVID-19 antigen card case and a test strip, which (one piece)/bag is composed of a sample pad, a conjugate pad (containing fluorescently labeled COVID-19 antibody and fluorescently labeled chicken IgY labeled antibody), a reaction pad, i.e., a nitrocellulose membrane (test line encapsulated with a COVID-19 antigen monoclonal antibody and a quality control line sheep anti-chicken IgY-coated antibody), an absorbent pad, and a PVC backing plate. 2 Sample extraction Phosphate buffer Bottle 25 solution 3 Extraction bottle / piece 25 4 Disposable / piece 25 sampling swab 5 SPECIFICATION / Parts 1

[0081] In addition, the present disclosure provides another embodiment:

[0082] The extraction bottle in the kit for detecting the COVID-19 antigen according to the present disclosure can be replaced with a single-lug tube.

[0083] The components, packaging and quantity of the kit (25 pieces/kit) are listed in Table 3.

TABLE-US-00003 TABLE 3 Composition, packaging and quantity of the kit Serial Specification number Component Main component (μL) Quantity 1 Test card for the This product is composed of a For one person 25 COVID-19 antigen card case and a test strip. The (one piece)/bag test strip is composed of a sample pad, a conjugate pad (containing a fluorescently labeled COVID-19 antibody and a fluorescently labeled chicken IgY labeled antibody), a reaction pad, i.e., a nitrocellulose membrane (a test line coated with a COVID-19 monoclonal antibody and a quality control line coated with a goat anti-chicken IgY coated antibody), an absorbent pad, and a PVC bottom plate. 2 Sample extraction Phosphate buffer Bottle 25 solution 3 Disposable sampling / piece 25 swab 4 SPECIFICATION / Parts 1

[0084] A method for testing a COVID-19 antigen using the kit as described above includes the following steps:

[0085] sampling a nasal mucosa fluid or an oral pharyngeal mucosa fluid by using a disposable sampling swab;

[0086] placing the sampling swab into a single-lug tube to which a sample extraction solution is added in advance, and sufficiently uniformly mixing the sample, such that the nasal mucosa fluid or the oral pharyngeal mucosa fluid remains in the single-lug tube; and

[0087] dropwise adding the sampled nasal mucosa fluid or oral pharyngeal mucosa fluid into the test card in the kit for testing, and determining a test result according to the test line and the quality control line.

[0088] The sampling specifically includes the following steps:

[0089] 1. sample collection: collecting the sample using an oral pharyngeal swab or a nasal pharyngeal swab;

[0090] 2. upon sampling, placing the disposable sampling swab into a single-lug tube containing the sample extraction solution, soaking the swab in the sample extraction solution and extrusively rotating the swab for 10 times to sufficiently mix the sample, and then extruding the swab over the surface of the solution such that the fluid in the swab remains in the tube as much as possible;

[0091] 3. connecting a disposable dropper to the single-lug tube containing the sample extraction solution;

[0092] 4. opening an aluminum foil bag, taking out the test card, and placing the test card on a dry and clean platform; and

[0093] 5. vertically dropwise adding the solution in the single-lug tube into the well in the test card, wherein due to operation differences, if, 2 min after 4 drops of the sample extraction solution is added, it is found through the observation window that no solution layer is precipitated, 1 more drop of the sample extraction solution is added to the corresponding well under the observation window; and

[0094] 6. within 10 to 15 min after sampling adding, determining and reading the test result on the test line and the quality control line by irradiating the observation window with the fluorescent flashlight, wherein the test result displayed after 30 min is of no clinical significance. In the fluorescence test, no matter whether it is negative or positive, the quality control line shall show a fluorescence band, and in this case, it is proved that the test result is valid.

[0095] It should be understood that described above are merely exemplary embodiments of the present disclosure, which are not intended to limit the projection scope of the present disclosure. The projection scope of the present disclosure shall be subject to the appended claims.